Canonical Allele Identifier: PA2827611887
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338426.1:p.Arg105Trp
CA5170399
NM_001351497.2:c.313C>T